Kume Tsutomu, Shackour Tarek
Feinberg Cardiovascular and Renal Research Institute, Northwestern University School of Medicine, Chicago 60611, IL, USA.
Oncotarget. 2018 Nov 27;9(93):36625-36630. doi: 10.18632/oncotarget.26358.
Aberrations in the expression of the transcription factor forkhead box C1 (FOXC1) have been linked to a number of malignancies. Here, we characterized the relationship between FOXC1 and cancer progression by conducting a meta-analysis of studies that reported the frequency of FOXC1 expression in tumors of different stages (T1, T2, T3, T4).
Relevant articles were retrieved from the Medline database by searching for the terms "FOXC1" and "cancer"; then, the retrieved articles were reviewed individually, and studies that were of multivariate cohort design, evaluated FOXC1 expression via immunohistochemical staining, and assessed the relationship between FOXC1 expression and cancer T-stage were included in our meta-analysis.
Our search terms identified 128 studies, 5 of which met all inclusion criteria. A total of 850 tumor samples were evaluated in the 5 studies; 452 samples were from early-stage (T1-T2) tumors, and 398 were from late-stage (T3-T4) tumors. FOXC1 was expressed in 60.7% (516/850) of all samples, in 54.6% (247/452) of early-stage tumor samples, and in 67.5% (269/398) of late-stage tumor samples. When calculated relative to early-stage samples, the pooled risk for FOXC1 expression in late-stage samples was 1.238 (95% CI = 1.061-1.444, = 0.007).
The results from our meta-analysis of 5 studies indicate that FOXC1 is 23.8% more likely to be expressed in late-stage tumors than in early-stage tumors.
转录因子叉头框C1(FOXC1)表达异常与多种恶性肿瘤相关。在此,我们通过对报告不同分期(T1、T2、T3、T4)肿瘤中FOXC1表达频率的研究进行荟萃分析,来描述FOXC1与癌症进展之间的关系。
通过在Medline数据库中搜索“FOXC1”和“癌症”检索相关文章;然后,对检索到的文章进行逐一审查,纳入多变量队列设计、通过免疫组织化学染色评估FOXC1表达并评估FOXC1表达与癌症T分期之间关系的研究进行荟萃分析。
我们的检索词共识别出128项研究,其中5项符合所有纳入标准。这5项研究共评估了850个肿瘤样本;452个样本来自早期(T1 - T2)肿瘤,398个样本来自晚期(T3 - T4)肿瘤。FOXC1在所有样本中的表达率为60.7%(516/850),在早期肿瘤样本中的表达率为54.6%(247/452),在晚期肿瘤样本中的表达率为67.5%(269/398)。相对于早期样本计算,晚期样本中FOXC1表达的合并风险为1.238(95%置信区间 = 1.061 - 1.444,P = 0.007)。
我们对5项研究的荟萃分析结果表明,FOXC1在晚期肿瘤中表达的可能性比在早期肿瘤中高23.8%。